BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 28065847)

  • 1. A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration.
    López Del Amo V; Palomino-Schätzlein M; Seco-Cervera M; García-Giménez JL; Pallardó FV; Pineda-Lucena A; Galindo MI
    Biochim Biophys Acta Mol Basis Dis; 2017 Mar; 1863(3):801-809. PubMed ID: 28065847
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial defects and neuromuscular degeneration caused by altered expression of Drosophila Gdap1: implications for the Charcot-Marie-Tooth neuropathy.
    López Del Amo V; Seco-Cervera M; García-Giménez JL; Whitworth AJ; Pallardó FV; Galindo MI
    Hum Mol Genet; 2015 Jan; 24(1):21-36. PubMed ID: 25122658
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Gdap1 knockout mouse mechanistically links redox control to Charcot-Marie-Tooth disease.
    Niemann A; Huber N; Wagner KM; Somandin C; Horn M; Lebrun-Julien F; Angst B; Pereira JA; Halfter H; Welzl H; Feltri ML; Wrabetz L; Young P; Wessig C; Toyka KV; Suter U
    Brain; 2014 Mar; 137(Pt 3):668-82. PubMed ID: 24480485
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Calcium Deregulation and Mitochondrial Bioenergetics in GDAP1-Related CMT Disease.
    González-Sánchez P; Satrústegui J; Palau F; Del Arco A
    Int J Mol Sci; 2019 Jan; 20(2):. PubMed ID: 30669311
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy.
    Barneo-Muñoz M; Juárez P; Civera-Tregón A; Yndriago L; Pla-Martin D; Zenker J; Cuevas-Martín C; Estela A; Sánchez-Aragó M; Forteza-Vila J; Cuezva JM; Chrast R; Palau F
    PLoS Genet; 2015 Apr; 11(4):e1005115. PubMed ID: 25860513
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Charcot-Marie-Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potential.
    Noack R; Frede S; Albrecht P; Henke N; Pfeiffer A; Knoll K; Dehmel T; Meyer Zu Hörste G; Stettner M; Kieseier BC; Summer H; Golz S; Kochanski A; Wiedau-Pazos M; Arnold S; Lewerenz J; Methner A
    Hum Mol Genet; 2012 Jan; 21(1):150-62. PubMed ID: 21965300
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Charcot-Marie-Tooth-related gene GDAP1 complements cell cycle delay at G2/M phase in Saccharomyces cerevisiae fis1 gene-defective cells.
    Estela A; Pla-Martín D; Sánchez-Piris M; Sesaki H; Palau F
    J Biol Chem; 2011 Oct; 286(42):36777-86. PubMed ID: 21890626
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Junctophilin-1 is a modifier gene of GDAP1-related Charcot-Marie-Tooth disease.
    Pla-Martín D; Calpena E; Lupo V; Márquez C; Rivas E; Sivera R; Sevilla T; Palau F; Espinós C
    Hum Mol Genet; 2015 Jan; 24(1):213-29. PubMed ID: 25168384
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Silencing of the Charcot-Marie-Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca2+ entry.
    Pla-Martín D; Rueda CB; Estela A; Sánchez-Piris M; González-Sánchez P; Traba J; de la Fuente S; Scorrano L; Renau-Piqueras J; Alvarez J; Satrústegui J; Palau F
    Neurobiol Dis; 2013 Jul; 55():140-51. PubMed ID: 23542510
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease.
    Niemann A; Ruegg M; La Padula V; Schenone A; Suter U
    J Cell Biol; 2005 Sep; 170(7):1067-78. PubMed ID: 16172208
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondria and calcium defects correlate with axonal dysfunction in GDAP1-related Charcot-Marie-Tooth mouse model.
    Civera-Tregón A; Domínguez L; Martínez-Valero P; Serrano C; Vallmitjana A; Benítez R; Hoenicka J; Satrústegui J; Palau F
    Neurobiol Dis; 2021 May; 152():105300. PubMed ID: 33582224
    [TBL] [Abstract][Full Text] [Related]  

  • 12. GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria.
    Pedrola L; Espert A; Wu X; Claramunt R; Shy ME; Palau F
    Hum Mol Genet; 2005 Apr; 14(8):1087-94. PubMed ID: 15772096
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondria-lysosome membrane contacts are defective in GDAP1-related Charcot-Marie-Tooth disease.
    Cantarero L; Juárez-Escoto E; Civera-Tregón A; Rodríguez-Sanz M; Roldán M; Benítez R; Hoenicka J; Palau F
    Hum Mol Genet; 2021 Jan; 29(22):3589-3605. PubMed ID: 33372681
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca
    González-Sánchez P; Pla-Martín D; Martínez-Valero P; Rueda CB; Calpena E; Del Arco A; Palau F; Satrústegui J
    Sci Rep; 2017 Feb; 7():42993. PubMed ID: 28220846
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations.
    Cassereau J; Chevrollier A; Gueguen N; Desquiret V; Verny C; Nicolas G; Dubas F; Amati-Bonneau P; Reynier P; Bonneau D; Procaccio V
    Exp Neurol; 2011 Jan; 227(1):31-41. PubMed ID: 20849849
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).
    Cassereau J; Chevrollier A; Gueguen N; Malinge MC; Letournel F; Nicolas G; Richard L; Ferre M; Verny C; Dubas F; Procaccio V; Amati-Bonneau P; Bonneau D; Reynier P
    Neurogenetics; 2009 Apr; 10(2):145-50. PubMed ID: 19089472
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene.
    Kabzinska D; Drac H; Rowinska-Marcinska K; Fidzianska A; Kochanski A; Hausmanowa-Petrusewicz I
    Acta Myol; 2006 Jun; 25(1):34-7. PubMed ID: 17039978
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The role of mitochondrial network dynamics in the pathogenesis of Charcot-Marie-Tooth disease.
    Palau F; Estela A; Pla-Martín D; Sánchez-Piris M
    Adv Exp Med Biol; 2009; 652():129-37. PubMed ID: 20225023
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A role for the GDAP1 gene in the molecular pathogenesis of Charcot‑Marie‑Tooth disease.
    Rzepnikowska W; Kochański A
    Acta Neurobiol Exp (Wars); 2018; 78(1):1-13. PubMed ID: 29694336
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Differential effects of Mendelian GDAP1 clinical variants on mitochondria-lysosome membrane contacts sites.
    Cantarero L; García-Vargas G; Hoenicka J; Palau F
    Biol Open; 2023 Apr; 12(4):. PubMed ID: 36912213
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.